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Human Disease and Mouse Model Detail
Human Disease

Term: Arthrogryposis, Distal, Type 2B; DA2B
OMIM ID: 601680

Synonyms Arthrogryposis Multiplex Congenita, Distal, Type 2B; Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities; Freeman-Sheldon Syndrome Variant; FSSV; Sheldon-Hall Syndrome; SHS
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Myh3 MYH3
Tnni2 TNNI2
Tnnt3 TNNT3
Tpm2 TPM2
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory